Article info
PDFDiagnostics
Original research
Molecular diagnoses in the congenital malformations caused by ciliopathies cohort of the 100,000 Genomes Project
- Correspondence to Dr Gabrielle Wheway, Department of Human Development and Health, University of Southampton Faculty of Medicine, Southampton, SO17 1BJ, UK; g.wheway{at}soton.ac.uk
Citation
Molecular diagnoses in the congenital malformations caused by ciliopathies cohort of the 100,000 Genomes Project
Publication history
- Received July 1, 2021
- Accepted August 27, 2021
- First published October 29, 2021.
Online issue publication
July 21, 2022
Article Versions
- Previous version (21 July 2022).
- Previous version (21 July 2022).
- You are viewing the most recent version of this article.
Supplementary Data
This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.
Supplementary Data
This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.
Request permissions
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Copyright information
© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.